US2185894A - Method of producing malleable iron - Google Patents
Method of producing malleable iron Download PDFInfo
- Publication number
- US2185894A US2185894A US186463A US18646338A US2185894A US 2185894 A US2185894 A US 2185894A US 186463 A US186463 A US 186463A US 18646338 A US18646338 A US 18646338A US 2185894 A US2185894 A US 2185894A
- Authority
- US
- United States
- Prior art keywords
- quenching
- graphite
- castings
- malleable iron
- malleableizing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 10
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 title description 9
- 229910001296 Malleable iron Inorganic materials 0.000 title description 9
- 238000010791 quenching Methods 0.000 description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 17
- 230000000171 quenching effect Effects 0.000 description 17
- 229910002804 graphite Inorganic materials 0.000 description 16
- 239000010439 graphite Substances 0.000 description 16
- 238000005266 casting Methods 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 229910001018 Cast iron Inorganic materials 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 229910000734 martensite Inorganic materials 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- 229910001037 White iron Inorganic materials 0.000 description 4
- 229910001566 austenite Inorganic materials 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 229910001567 cementite Inorganic materials 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- 238000005087 graphitization Methods 0.000 description 4
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- 239000002826 coolant Substances 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 238000005496 tempering Methods 0.000 description 3
- 238000007792 addition Methods 0.000 description 2
- 238000000137 annealing Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 235000019227 E-number Nutrition 0.000 description 1
- 239000004243 E-number Substances 0.000 description 1
- 244000228957 Ferula foetida Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 229910001562 pearlite Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D5/00—Heat treatments of cast-iron
- C21D5/04—Heat treatments of cast-iron of white cast-iron
- C21D5/06—Malleabilising
Definitions
- the cast iron should have such a composition that castings of the dimensions and'shape required can be made largely martensitic by quenching without the formation of quenching cracks.
- suitable alloy additions such as Mn, Ni, Cr, Mo etcetera
- the hardening depth of steel and cast iron can be raised to such an extent that even heavy objects may be through-hardened on quenching in oil or even on cooling in air, thus preventing the formation of quenching cracks.
- composition should be balanced in regard to tendency for graphitization, i, e. the castings, of required size and under existing casting conditions, should solidify white, with prac tically no graphite formation but graphite nuclei should readily form on tempering of the martensite and their growth on annealing should not be retarded or suppressed.
- C, Si, Ni and Cu favour graphitization, Mn, Cr and Mo retard it.
- condition (2) i. e. the C and Si contents will, in the presence of the low Mn content, produce the desired graphitization tendency.
- condition (1) canbe brought about in different ways, for instance:
- the process for producing malleable iron for which patent is herewith applied consists in taking castings of a cast iron containing certain alloy components, on one hand at least one of such components as favour the graphitization, for instance, Si,-Ni, Cu, on the other at least one of such alloy components as increase the depth of hardening on quenching or cooling, for instance, Ni, Cr, Mn, in such concentrations that with existing dimensions and casting conditions, the castings solidify white and, further, can be hardened to suflicient depth to a largely martensiticaustenitic state by cooling from a temperature exceeding A1 in oil or equivalent or less eflicacious cooling medium, and subjecting said castings first to cooling in a cooling medium at most as efficacious as oil from a temperature exceeding A1 so as to transform the matrix into a largely martensitic-austenitic state, and then to a malleableization or cooled at a faster rate than ordinarily during the later stage of the malleableizing anneal.
- the heat-treatment may consist in fairly rapid cooling from a temperature above A1 to give a pearlitic or sorbitic matrix or in quenching in oil or the like from a temperature above A1 to give martensitic structure followed by tempering to a temperature below A1.
- tempering may be omitted or carried out at a low temperature.
- Method of producing malleable iron from cast iron comprising making castings of white cast iron, containing a component increasing the depth of hardening taken from a group consisting of nickel, chromium and manganese, said component being in such concentration that the other hand a subsequent or concluding heatcastings will be hardened to suflicient depth to a largely martensitio-austenitic state by cooling from a temperature exceeding A1 in a cooling medium not more efficacious than oil, and subjecting the castings to such a cooling and then to a malleableizing anneal.
- heating the heat-treated object, prior to the malleableizing anneal up to about 600 C. at a rate not exceeding 20 per minute.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Heat Treatment Of Articles (AREA)
Description
Patented Jan. 2, 1940 METHOD OF PRODUCING MALLEABLE IRON Axel Gustaf Emanuel Hultgren, Djursholm,
Sweden No Drawing. Application January 22, 1938, Se-
rial No. 186,463. In Sweden January 25, 1937 3 Claims.
According to the so-called American process malleable iron is produced from white cast iron of suitable composition in the following manner. The castings are first annealed at a temperature formed in the cementite, but in the martensite that constitutes a great part of the matrix after quenching, the remainder of the matrix being austenite. On heating-tempering-rnartensite above AC1, usually between 800 and 900 C. until it is usually decomposed into an aggregate of fer- 5 all free cementiteFesC-is consumed, i. e. unrite and cementite. In this case, i. e. on tempertil the original structure consisting of austenite ing hardened cast iron, of the composition comand cementite has been transformed into austenmonlyused for malleable castings, numerous subite and graphite, and are then allowed to cool microscopic graphite particles are also formed slowly, the temperature being usually kept mm which on continued heating to higher tempera- 10 stant, somewhat below An, for an extended tures grow to particles visible in the microscope. period. Owing to the slow cooling, the amount These particles act as nuclei for the precipitation of carbon that corresponds with the decreasing of graphite during the malleableizing anneal. solubility is precipitated as graphite, not as ce- Owing to the numerous graphite particles formed mentite. While the temperature is held below the malleableizing anneal, under favourable con- 16 An, the pearlite formed from austenite at Ari is ditions can be shortened to such an extent that decomposed into ferrite and graphite. Thus, the the whole process, including quenching, takes less end product, malleable iron, consists of ferrite than 12 hours. On quenching followed by rapid with particles of graphite distributed in it. For heating the number of graphite particles formed 20 the whole process several days are required. during malleableizing-as counted in unit area 20 Several years ago, two Japanese investigators, was multiplied more than 100 times as compared D. Saito and H. Sawamura, discovered the fact with the number formed on ordinary malleableizthat, on first quenching the-castings in water. ing treatment, If the heating after quenching from a high temperature, about 850-950 C., and was retarded the number was doubled again.
then tslilibjecting them to the malleableizing an- This is seen from the following figures: 25 neal, e number of graphite particles formed are o reatly increased and, in consequence the annealor} q 8 wlthout PIE-quenching treatment can be considerably shortened, say. pal 1c es P On quenching from 975 followed by rapid heatto less than 48 hours. This 18 described in in and malleableizing at C about 14 000 I Memoirs of the College of Engineering, Kyoto paiticlespm sq mm 30 Impeml 1927 On quenching from 975 (2., rapid heating to 600 under the title. A New Phenomenon Concerning C h o 1 olding at 600 C. for /2 hour and mallethe uraphitization of White Cast Iron and Its ableizm at C about 20 000 articles pro Application to the Manufacture of Black. Heart sq p Malleable Castings." The authors explain the o 35 phenomenon by assuming that the stresses proon quenching from 8 slow heatmg to 600 C., holding at 600 C. for hour and malleduced on the transformation of austenite into am izin t C about 30 000 articles m martensite cause the cementite particles to be e g a p p broken up into small fragments, in the free sur- 40 faces of which graphite nuclei are readily formed These results were obtained on 6 mm. rd. rods 40 during the subsequent annealing treatment. of white cast iron having the following comp Their hypothesis appears to be supported by the tion: 3.0% C, fact that the result described is obtained after 0.05% S. The rods were que n Oil and very rapidcooling only. The practical developthen'became martensiticment of this process, anticipated from the re- If this proc is pplied to castin f whi is duced cost of 'manufacture, has not, however, cast iron of ordinary analysis similar to the above been realized. and having the dimensions usually required for The present invention developed out of an inmalleable castin it fails for the following renvestigation carried out by the inventor with 9. sons: eith r q hing is doneinoil, 111, whi
view to ascertain the conditions required for case the matrix becomes sorbitic and the graphite 5 shortening the malleableizing anneal by a previparticles formed 11 nn lin are not increased ous quenching treatment. It was found that the in numb r (2) quenching is (10118 in in hypothesis put forth by Saito and Sawamura for which case quenching cracks cannot be avoided. explaining the formation of numerous graphite Thus, in order that the discovery ma er finuclei is not correct. ese nuclei are not ing the imiwrtanceo an. nslte asatrix for enhanced graphite nucleation maybe put to practical application the following conditions must be fulfilled.
(1) The cast iron should have such a composition that castings of the dimensions and'shape required can be made largely martensitic by quenching without the formation of quenching cracks. By the use of suitable alloy additions, such as Mn, Ni, Cr, Mo etcetera, the hardening depth of steel and cast iron can be raised to such an extent that even heavy objects may be through-hardened on quenching in oil or even on cooling in air, thus preventing the formation of quenching cracks.
(2)- The composition should be balanced in regard to tendency for graphitization, i, e. the castings, of required size and under existing casting conditions, should solidify white, with prac tically no graphite formation but graphite nuclei should readily form on tempering of the martensite and their growth on annealing should not be retarded or suppressed. C, Si, Ni and Cu favour graphitization, Mn, Cr and Mo retard it.
A common composition for making malleable iron is mentioned above. This is balanced in the sense of condition (2), i. e. the C and Si contents will, in the presence of the low Mn content, produce the desired graphitization tendency. The changes required in order to fulfil condition (1) canbe brought about in different ways, for instance:
After the various ways of' carrying out the invention have thus been defined in principle, the
actual amounts of the respective alloy contents to be applied in each particular case are easily found by experiment, at the same time taking into consideration the cost and'physical and chemical properties of the malleable iron produced.
The process for producing malleable iron for which patent is herewith applied consists in taking castings of a cast iron containing certain alloy components, on one hand at least one of such components as favour the graphitization, for instance, Si,-Ni, Cu, on the other at least one of such alloy components as increase the depth of hardening on quenching or cooling, for instance, Ni, Cr, Mn, in such concentrations that with existing dimensions and casting conditions, the castings solidify white and, further, can be hardened to suflicient depth to a largely martensiticaustenitic state by cooling from a temperature exceeding A1 in oil or equivalent or less eflicacious cooling medium, and subjecting said castings first to cooling in a cooling medium at most as efficacious as oil from a temperature exceeding A1 so as to transform the matrix into a largely martensitic-austenitic state, and then to a malleableization or cooled at a faster rate than ordinarily during the later stage of the malleableizing anneal. In making pearlitic malleable iron alloy cast iron is often employed. In that case, the object of the alloying additions is different from that of the present inventionand the heat-treatment succeeds malleableization instead of preceding it as described above. On the treatment may also be applied to castings that have been manufactured or treated according to the present invention, with the object of obtaining greater strength. The heat-treatment may consist in fairly rapid cooling from a temperature above A1 to give a pearlitic or sorbitic matrix or in quenching in oil or the like from a temperature above A1 to give martensitic structure followed by tempering to a temperature below A1. When abrasive resistance combined with the lubricating properties of graphite are called for tempering may be omitted or carried out at a low temperature.
Having now described my invention, what I claim as new and desire to secure by Letters Patent is:
1. Method of producing malleable iron from cast iron, comprising making castings of white cast iron, containing a component increasing the depth of hardening taken from a group consisting of nickel, chromium and manganese, said component being in such concentration that the other hand a subsequent or concluding heatcastings will be hardened to suflicient depth to a largely martensitio-austenitic state by cooling from a temperature exceeding A1 in a cooling medium not more efficacious than oil, and subjecting the castings to such a cooling and then to a malleableizing anneal.
2. In a method claimed in claim 1, heating the heat-treated object, prior to the malleableizing anneal, up to about 600 C. at a rate not exceeding 20 per minute.
3. In a method claimed in claim 1, subjecting the heat-treated object to heating prior -to the malleableizing anneal, the object being kept within a range of temperature of between 550 and 700 for more than 10 minutes.
AXEL GUSTAF HULTGREN.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE2185894X | 1937-01-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2185894A true US2185894A (en) | 1940-01-02 |
Family
ID=20424905
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US186463A Expired - Lifetime US2185894A (en) | 1937-01-25 | 1938-01-22 | Method of producing malleable iron |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2185894A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2438267A (en) * | 1942-03-23 | 1948-03-23 | Timken Roller Bearing Co | Graphitic steel |
| US2556408A (en) * | 1946-12-19 | 1951-06-12 | Wurlitzer Co | Accordion bass section |
| US2887421A (en) * | 1955-01-05 | 1959-05-19 | Renault | Method of producing castings having high mechanical properties |
| US2895860A (en) * | 1955-08-05 | 1959-07-21 | Renault | Pressure chill-castings of iron |
| US2895859A (en) * | 1954-08-04 | 1959-07-21 | Renault | Process for the manufacture of piston rings |
| US2899346A (en) * | 1959-08-11 | Cast iron heat | ||
| US2901386A (en) * | 1952-02-18 | 1959-08-25 | Renault | Method of heat treating cast iron |
| US2901384A (en) * | 1952-02-20 | 1959-08-25 | Renault | Method for treating cast iron castings |
| US2906653A (en) * | 1955-02-01 | 1959-09-29 | Renault | Die-casting of iron in chill-moulds |
| US2906651A (en) * | 1952-02-21 | 1959-09-29 | Renault | Method for producing malleabilized castings |
| US2992950A (en) * | 1953-11-18 | 1961-07-18 | Renault | Malleable cast iron compositions |
| US3013911A (en) * | 1953-11-18 | 1961-12-19 | Renault | Malleable cast iron compositions |
| US3360407A (en) * | 1964-04-30 | 1967-12-26 | Teves Thompson & Co G M B H | Cast-iron composition of high refractoriness and strength and process for making same |
| US20060144478A1 (en) * | 2003-02-12 | 2006-07-06 | Nippon Steel Corporation | Cast iron billet excelling in workability and process for producing the same |
-
1938
- 1938-01-22 US US186463A patent/US2185894A/en not_active Expired - Lifetime
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2899346A (en) * | 1959-08-11 | Cast iron heat | ||
| US2438267A (en) * | 1942-03-23 | 1948-03-23 | Timken Roller Bearing Co | Graphitic steel |
| US2556408A (en) * | 1946-12-19 | 1951-06-12 | Wurlitzer Co | Accordion bass section |
| US2901386A (en) * | 1952-02-18 | 1959-08-25 | Renault | Method of heat treating cast iron |
| US2901384A (en) * | 1952-02-20 | 1959-08-25 | Renault | Method for treating cast iron castings |
| US2906651A (en) * | 1952-02-21 | 1959-09-29 | Renault | Method for producing malleabilized castings |
| US2992950A (en) * | 1953-11-18 | 1961-07-18 | Renault | Malleable cast iron compositions |
| US3013911A (en) * | 1953-11-18 | 1961-12-19 | Renault | Malleable cast iron compositions |
| US2895859A (en) * | 1954-08-04 | 1959-07-21 | Renault | Process for the manufacture of piston rings |
| US2887421A (en) * | 1955-01-05 | 1959-05-19 | Renault | Method of producing castings having high mechanical properties |
| US2906653A (en) * | 1955-02-01 | 1959-09-29 | Renault | Die-casting of iron in chill-moulds |
| US2895860A (en) * | 1955-08-05 | 1959-07-21 | Renault | Pressure chill-castings of iron |
| US3360407A (en) * | 1964-04-30 | 1967-12-26 | Teves Thompson & Co G M B H | Cast-iron composition of high refractoriness and strength and process for making same |
| US20060144478A1 (en) * | 2003-02-12 | 2006-07-06 | Nippon Steel Corporation | Cast iron billet excelling in workability and process for producing the same |
| EP1595964A4 (en) * | 2003-02-12 | 2009-09-23 | Nippon Steel Corp | CAST IRON BARRIER WITH EXCELLENT WORKABILITY AND MANUFACTURING METHOD THEREFOR |
| US20100172784A1 (en) * | 2003-02-12 | 2010-07-08 | Nippon Steel Corporation | Cast iron semi-finished product excellent in workability and method of production of the same |
| US8302667B2 (en) | 2003-02-12 | 2012-11-06 | Nippon Steel Corporation | Cast iron semi-finished product excellent in workability and method of production of the same |
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